A method for determining the proper configuration of a fixator or other medical device to correct a given deformity by solving the simultaneous equations representing the kinematic chain for the device. One skilled in the art would appreciate that x-rays, clinical evaluations, or a combination of both may be used to determine the distal and proximal mounting characteristics, including the use of digital x-rays with images from an imaging device to reduce or eliminate the needs for a physician to take measurements. The technique can be expanded to other medical evaluations. Additionally, one skilled in the art would appreciate that the method of the present invention could be written as one or more sets of instructions stored on a computer-readable medium that could be executed by a computer.
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1. A method for determining a transform of a deformity-correcting fixator in a treatment plan to treat a bone condition, the method comprising the steps of:
generating a first two-dimensional digital x-ray image comprising a first plurality of identifiable shapes associated with the deformity-correcting fixator;
generating a second two-dimensional digital x-ray image comprising a second plurality of identifiable shapes associated with the deformity-correcting fixator, the second digital x-ray image taken at an angle relative to the first digital x-ray image;
in a computer, characterizing a mounting condition for a first bone fragment attachment apparatus of the deformity correcting fixator and a second bone fragment attachment apparatus of the deformity correcting fixator based on the first and second images, wherein characterizing a mounting condition includes
a) calculating a three-dimensional coordinate system to relate the deformity correcting fixator to the bone, comprising:
i) automatically identifying outlines of the first and second pluralities of identifiable shapes and determining size of the identifiable shapes in the first and second two-dimensional digital x-ray images,
ii) scaling the first and second two-dimensional digital x-ray images by comparing the determined size of the identifiable shapes in the first and second two-dimensional digital x-ray image to pre-stored size values corresponding to the actual size of the shapes of the identifiable shapes associated with the deformity-correcting fixator,
iii) identifying a reference origin of the deformity correcting fixator in each of the first and second two-dimensional digital x-ray images based on the scaled identifiable shapes in order to relate the first plurality of identifiable shapes in the first two-dimensional digital x-ray image to the second plurality of identifiable shapes in the second two-dimensional digital x-ray image, and
iv) generating the three-dimensional coordinate system based on the location of the reference origin and the location of two or more of the additional identifiable shapes,
b) characterizing a transform of first and second bone fragments for comparison to the deformity correcting fixator comprising:
i) receiving an input representing a first line extending along a first bone fragment in the first two-dimensional digital x-ray image,
ii) generating an equation for a first plane perpendicular to the first line extending along the first bone fragment,
iii) receiving an input representing a second line extending along the first bone fragment in the second two-dimensional digital x-ray image,
iv) generating an equation for a second plane perpendicular to the second line extending along the first bone fragment,
v) calculating an intersection of the first plane and the second plane to identify a line co-linear with a reference axis of the of the first bone fragment,
vi) repeating steps i) to v) for the second bone fragment to identify a line co-linear with the reference axis of the second bone fragment,
c) establishing a first transform between at least one of the first and second bone fragments and at least one of the first and second bone fragment attachment apparatuses of the deformity correction fixator, the first bone fragment attachment apparatus being fixed relative to the first bone fragment and the second bone fragment attachment apparatus being fixed relative to the second bone fragment in the three-dimensional coordinate system, and
calculating a set of fixator settings corresponding to a desired second transform of the first bone fragment relative to the second bone fragment with the established first transform.
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8. The method of
determining an axial rotation for the first bone fragment attachment apparatus;
determining an anterior-posterior rotation for the first bone fragment attachment apparatus;
determining a lateral rotation for the first bone fragment attachment apparatus;
determining a pin offset for the first bone fragment attachment apparatus; and
determining the bone length.
9. The method of
identifying a center for each identifiable shape of the first plurality of identifiable shapes;
identifying unit vectors for each identifiable shape of the first plurality of identifiable shapes; and
determining said reference origin by generating a solution to equations representing the identified unit vectors.
10. The method of
11. The method of
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17. The method of
iteratively calculating successive sets of fixator settings using the first transform and prior sets of fixator settings to yield a set of fixator settings resulting in the desired transform aligning the first and second bone segments.
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This non-provisional patent application claims priority under 35 U.S.C. §119 to U.S. Provisional Patent Application No. 60/426,439, titled Unilateral Fixator Method, filed Nov. 14, 2002. This provisional application is hereby fully incorporated herein by reference.
The present invention relates to a method for using a fixator device and more specifically to developing a prescription for adjusting a fixator for deformity correction and for characterizing tissue through non-evasive methods.
In orthopedic medicine, physicians often need to correct certain skeletal injuries or deformities with external fixator devices. These devices use pins or wires attached to the separate bone segments and an external structural frame to align, or fix, the bone segments in a way to aid in repairing the injury or correcting the deformity. Often the physician must gradually adjust the orientation of the bone segments over time, optimally with the capability to adjust the orientation along six degrees of freedom to ensure the bone segments are placed in the correct anatomic condition.
Devices and methods for treating musculoskeletal deformities are well known in the art. Although these devices vary considerably in design, they typically fall into two broad categories, circular ring and unilateral devices. The circular ring device category is exemplified by Ilizarov-type systems, which have two rings connected by linear struts with a fixed or hinged connection at each end of each strut. A device called a space frame, which has two rings connected by six linear struts having a spherical joint at each end arranged in a hexapod configuration, e.g., a Stewart frame, represents an advancement on the original Ilizarov concept.
The Ilizarov device is constructed based on the deformity that needs correcting, that is, for a specific patient and a specific deformity on that patient, hinges and struts are added to address each degree of deformity in a specific case. Ilizarov-type devices are often referred to as serial manipulators in that each adjustment relates to a single degree of deformity. This approach requires the frame to be constructed based on the deformity present, resulting in a fairly straightforward method of use but a potentially complex set of multiple and potentially endless configurations. The space frame is a device that conceptually comes in one configuration even though rings and struts can be of differing sizes. The Stewart frame-type space frame is often referred to as a parallel manipulator in that any given adjustment to any of the six struts will result in a change to all six degrees of freedom. This characteristic makes the Stewart-frame type device less intuitive to use and a computer program is often required to direct the user in making the adjustments to correct the deformity.
The unilateral device category has several devices that basically consist of a series of orthogonal planar hinges or spherical joints and, in some cases, sliders that can be locked into a particular orientation. Typically these devices can be used to fix bone segments in a particular orientation but not to gradually adjust the orientation, since the joints of the device do not have a direct adjustment device associated with each hinge or slider. Instead, the joints of the device must be loosened and then grossly manipulated on the device as a whole. Like the Ilizarov-type circular ring fixators, these devices often need to be constructed or mounted in a particular orientation depending on the characterization of the deformity. This requirement complicates their use and also necessitates multiple configurations to address the range of deformities that physicians typically encounter.
An innovative unilateral fixator, described in U.S. Non-Provisional patent application Ser. No. 10/664,769, entitled Unilateral Fixator, incorporated herein by reference, provides a six-degree-of-freedom manipulator in the form of an open kinematic chain, similar to many industrial robot arms in use today. At the start of the kinematic chain is the connection to what would be the reference bone segment, otherwise known as the ground. At the end of the kinematic chain is the connection to what would be the moving bone segment. Each of the links in the kinematic chain is made up of a rigid structural member with the connection between links being the joints.
The positioning and adjusting of a fixator, such as a six-degrees-of-freedom unilateral fixator described in U.S. Non-Provisional patent application Ser. No. 10/664,769 allows a physician to correct a deformity. The starting point for determining the positioning and adjusting of the fixator includes x-rays that depict a given deformity. Typically, measurements such as the axial rotation, the anterior-posterior (AP) rotation, the lateral rotation, the pin offset, and bone length, are used to position and adjust a fixator. A physician may make these measurements directly on x-rays of a deformity. Although this technique is adequate for characterizing a deformity, these manual measurements do require increased work for a physician and may introduce error. An improved method would take advantage of digital imaging to reduce or eliminate the need for manual measurements.
What is needed is a method of deformity characterization and description of the relative mounting orientation of a deformity-correcting fixator device relative to the deformity such that a mathematical transform can be obtained is needed. Optimally, the method would minimize measurements taken by a physician. Also, the method may be adaptable to characterizing any type of tissue configuration captured on an x-ray.
The present invention provides a method for transforming readily available orthopedic data into parameters to configure a fixator to achieve a needed or desired orientation of the bone segments, by solving a system of simultaneous equations represented by a kinematic chain for a fixator device that provides six degrees of freedom of movement, either an open kinematic or closed kinematic chain. Advantageously, this system provides a method for manipulating a fixator with six degrees of freedom that can correct, through both gross and fine adjustments, bone deformities in any direction. One aspect of the invention includes a method for extracting data from an x-ray that greatly reduces or eliminates the need for a physician to perform manual measurements.
One aspect of the present invention provides a method for determining a position of a deformity-correcting fixator. The steps of the method include (1) characterizing a mounting condition for a proximal bone fragment attachment apparatus and a distal bone fragment attachment apparatus; (2) determining a first set of fixator settings and characteristics corresponding to the physical orientation and characteristics of the fixator; (3) determining a deformity correction matrix by solving a plurality of simultaneous equations corresponding to kinematic equations for the fixator; and (4) solving for a second set of fixator settings by equating the deformity correction matrix to a deformity correction transform. In this aspect, the mounting conditions may be characterized using manual measurements.
In another aspect of the invention, an imaging device may be used to place an image on at least two digital x-rays to characterize tissue captured in the x-ray, including the steps of (1) projecting an image from an imaging device onto an x-ray, wherein the x-ray contains the tissue and the imaging device includes at least three balls; (2) generating a digital computer-readable file of the x-ray; (3) detecting the edge of images on the digital file of the x-ray; (4) discovering possible circular outlines from images; (5) determining the radius and center associated with the possible circular outlines; (6) determining one or more anatomical axes associated with the tissue; (7) characterizing the coordinate system associated with the imaging device; and (8) characterizing the physical configuration of the tissue. In one exemplary embodiment, the tissue represents bone fragments to be corrected by a fixator. This aspect can be used to replace manual measurements for characterizing mounting conditions of a fixator.
The aspects of the present invention may be more clearly understood and appreciated from a review of the following detailed description of the disclosed embodiments and by reference to the drawings and claims.
Exemplary embodiments of the present invention provide a method for defining the manipulation of a fixator device and for characterizing tissue, such as bone fragments, which may be acted upon by the fixator.
Attached to each of the first and second compound movable joint 110, 120 is a clamp plate 160 and a clamp body 170. These clamp plates 160 and clamp bodies 170 receive pins or other suitable devices for attaching the first and second compound moveable joints 110, 120 to a patient's body, and more specifically to segments of a bone (not shown). Each clamp plate 160 is secured to its corresponding clamp body 170 with a plurality of cap screws, such as screw 180. Each cap screw 180 may be threaded into a combination of holes in the clamp plate 160 and the clamp body 170 such that cap screws 180 straddle each pin.
One skilled in the art will appreciate that the exemplary method described below could be used for any deformity-correcting fixator that provides for six degrees of freedom, such as a ring fixator, and is not limited to the exemplary unilateral fixator presented in
The current invention includes a method for translating clinical measurements into device parameters that establish the proper orientation of each segment revolute joint 122, 124, 126, 128 and the length of the strut structure. The fixator device is attached through pins and pin claps, or similar connecting structures, to two bone fragments that comprise the bone deformity. The device may then be manipulated, that is, moved, such that the bone fragments are aligned in a desired position. This alignment may be changed over time to complete the deformity correction process. One of the bone fragments will be a reference fragment. The other fragment, the moving fragment, will be moved to align with the reference fragment.
One skilled in the art will appreciate that the method of the present invention could be written as one or more sets of instructions stored on a computer-readable medium that could be executed by a computer. This computer may include a memory storage device; one or more computer processing units; input devices, such as a keyboard and pointing device such as a mouse; a monitor; and other peripheral devices.
At step 220, the physical characteristics and initial settings of the device are determined. These characteristics and settings comprise both fixed and variable input values. The fixed values relate to the hard dimensions of the fixator device, that is, values that are constant for a given fixator. The variable inputs are the settings of the adjustments of the device. The fixed values include the following (where the terms “reference” and “moving” refer to the bone fragment attached to the compound movable joint):
The variable values, which are solved for in the manipulation calculation process, include the following (where the terms “reference” and “moving” refer to the bone fragment attached to the compound movable joint):
At step 230, the deformity correction is determined. This determination is based on successive solving of the simultaneous equations comprising the kinematic chain equations for a fixator device. The five equations related to an exemplary embodiment are provided below, along with the definition of the matrixes that form the equation variables. Some of the variables are described below, in connection with
A=Masc
B=Masc
C=Masc
D=Masc
E=Masc
where,
At step 240, a deformity transform is calculated. This transform equates the solution to the kinematic chain equations to a desired deformity matrix, allowing for the solution of the variables associated with each of the revolute joints 122, 124, 126, 128 in the exemplary fixator. The following equation is used:
In other words, the product of the five matrixes represented by the designations A, B, C, D, and E, presented above, is set equal to the desired deformity transform. The deformity transform presented above is an augmented identity matrix. One skilled in the art would appreciate that the desired deformity matrix does not have to be an augmented identity matrix. Instead, the desired deformity transform can include a prescribed residual deformity.
At step 250, the fixator device position is set, based on the solution for the set of variable values at step 240. At step 260, if adjustments over time are needed, the process 200 returns to step 210 and repeats. In this case, the “initial device settings” at step 220 are the current settings for the device, that is, the settings determined at step 250. When no additional adjustments are needed, the process 200 ends.
At step 320, the AP rotation for the proximal pins is determined. With the proximal pins lying in a plane parallel to the view plane, the magnitude of the AP rotation for the proximal mounting is observed with respect to the proximal fragment anatomic axis and a line normal to the proximal pins. Image 420 depicts this measurement.
At step 330, the lateral (lat) rotation for the proximal pins is determined. With the face plane of the proximal clamp assembly normal to the view plane, the magnitude of the lateral rotation for the proximal mounting is observed. Image 430 depicts this measurement.
At step 340, the proximal pin offset is determined. With the face plane of the proximal clamp assembly normal to the view plane, the pin offset is measured from the center of the proximal clamp assembly to the anatomic axis of the fragment attached to the proximal pin set. Image 440 depicts this measurement.
At step 350, the process 210a determines If the characterization of mounting conditions has been done for both the proximal and distal pin sets. If not, the process 210a returns to step 310 and is repeated through step 340. When, at step 350, it is determined that the mounting conditions for both the distal and proximal pin sets have been completed, the process 210a proceeds to step 360.
At step 360, the bone length is determined. The bone length is the distance along the anatomic axis between the proximal and distal mounts. Image 440 depicts this measurement.
One skilled in the art would appreciate that the process could begin with the distal pin set and be repeated for the proximal pin set. Alternatively, the proximal and distal characterizations could take place at the same time. For example, at step 310, the axial rotation for both the distal and proximate pin sets could be determined prior to moving to step 320 and so on. Also, one skilled in the art would appreciate that the five characterizations performed for both the distal and proximal pin sets could be performed in any order.
Referring to
One skilled in the art would appreciate that oblique x-rays, rather than AP and lateral x-rays could be taken. This different geometry would need to be considered in implementing the method as described below. Also, shapes other than spheres may be used in an imaging device or the shapes can be eliminated, with the ends of the posts serving as points that are located on the digital x-rays. The digital x-ray processing would then be altered to locate the projection of the used shape on the digital x-ray images.
The prior art includes a technique for employing stereoscopic infrared cameras to determine the location of a surgeon's instrument by including on that instrument three orthogonally-opposed posts with balls on each end and a fourth ball at the point where all three posts are joined. The present invention can be distinguished from this prior art. The prior art technique employs a computer-generated image of tissue that the surgeon is acting on. This image is based on typical parameters for a patient. Unlike the prior art technique, the present invention employs actual images of bone fragments, since “typical” fractures or deformities do not exist. Also, the surgical technique of the prior art relies on the reflectivity of the balls to infrared light to allow the imaging system to “see” the instrument as it moves. In the present invention, the balls are used to form images on a digital or digitized x-ray, or similar image of a fracture or deformity, or other tissue mass, to characterize the tissue mass based on the know configuration of the balls on the imaging device.
At step 510, initial input settings are established. At this step, the digital images of x-rays are read by a computer, the characteristics of the projected images are set, and digital image processing set-up is established. These processes provide input parameters used in the later evaluation of the x-ray images. This step is discussed in greater detail below, in conjunction with
At step 520, the edges of images on the digital x-rays are determined. That is, the edges for the individual shapes that make up the entire x-ray image are determined. These shapes may correspond to the imaging device, the fixator device, or the tissue, such as bone fragments. Each pixel within each of the x-ray bitmap images are evaluated with respect to the intensity values contained in adjacent pixels. If the ratio of the intensity of adjacent pixels is less than a specified slope value, then the pixel value is set to the maximum intensity (255). Conversely, if the ratio of the intensity of adjacent pixels is greater than a specified slope value, the pixel value is set to the minimum intensity (0). This process highlights the edges within the x-ray images, that is, maximizes the intensity of the edges of all images on the digital x-rays and minimizes the intensity of other parts of the image.
At step 530, possible circle outlines within the digital x-ray image are identified. In other words, each of the individual images that make up the entire x-ray image is evaluated to determine if that image represents a circle. In this exemplary embodiment, three balls of different size are attached to the end of three orthogonal segments to form a device used to project images onto the x-rays, an imaging device. One of these devices is attached to both the distal and the proximal ends of the exemplary unilateral fixator at the pin clamps. When x-rays from an x-ray source pass through the imaging device, circular shadows, or images, are generated on the overall x-ray image. The x-rays also pass through the soft and hard tissue, such as bone fragments, and, possibly, the fixator, and all of these structures may cause images to be formed on the overall x-ray image. The circular images can then be used to characterize the bone fragments or other tissue mass relative to the fixator device.
To scan the image for outlines that could represent the circular shadows of the balls representing the axis of the coordinate systems attached to each clamp assembly, an algorithm is used to step through an image matrix at a given increment. Each digital x-ray image is divided into a grid system of rows and columns. A starting point is selected as a central pixel from which a search is conducted in the horizontal and vertical direction to identify the next pixel having a maximum value (255). That is, the search attempts to identify the pixels the image edges, in the up, down, left and right direction. If the central pixel is itself at a maximum value (255), in other words, is on an edge, then that pixel is skipped. In addition, if while scanning in any given direction the number of pixels scanned over exceeds a maximum diameter setting for the circle being searched for, that central pixel is skipped. The maximum diameter is an input parameter to the process and represents the largest diameter a circular shadow corresponding to the imaging device may have on the digital x-ray image.
Each pixel of the digital x-ray image is scanned in sequence. This sequence may move horizontally or vertically along the digital x-ray image to consecutive pixels or may be random. Once the entire image is scanned, the central pixel locations along with the four pixels corresponding to the up, down, left and right edges for each central pixel are stored on a computer storage device in a table of values for each digital x-ray image.
At step 540, possible circular images are characterized, in terms of radius and center location. In other words, each individual images on the overall digital x-rays identified as possibly being a circular image corresponding to the projection of a ball on an imaging device, is evaluated to determine if the image is indeed a circle. This step is described in greater detail below, in conjunction with
At step 550, the circular images identified at step 540 are superimposed onto the digital x-ray images. That is, the images calculated at step 540 are placed on the digital x-ray images by a computer. This process may include generating circles with the characteristics determined at step 540 on the digital x-ray image in a way that distinguishes these superimposed circular images from any original images on the overall digital x-ray image. This step is used to confirm that the circular images identified at step 540 represent the circular shadows on the x-rays of the balls that describe the imaging device attached to each pin clamp assembly.
At step 560, the anatomical axes of the bone fragments are determined. At step 570, the proximal and distal coordinate systems are characterized. The terms “proximal” and “distal” relate to the relative positions of the clamp assembles on the exemplary fixator. At step 580, the positions of the bone fragments are characterized. These steps are described in greater detail below, in association with
At step 620, the imaging device data input is determined. In this embodiment, the imaging device contains balls and rods. As discussed above, an exemplary device includes three balls, each rod having a ball attached to one end and with the other ends of the three rods joined together at a point referred to as the origin. One device is attached to each end of an exemplary fixator 100 (
One skilled in the art would appreciate that other device configurations may be used. One such configuration would include a fourth ball at the origin point, that is, the point where all three rods are joined. This configuration would allow the origin to be projected onto the x-ray image, simplifying the evaluation of the x-ray image, as discussed below. However, this configuration would also add an additional circular image on the x-ray, perhaps cluttering the overall digital x-ray image and making the identification of the individual circular images more difficult.
Similarly, one skilled in the art would appreciate that the two devices used in this example each could have different size balls, for a total of six different size balls, to facilitate discriminating between the circular images on the x-ray. Also, a single device could be used, attached to the fixator at a point. In this case, device input would also include the original settings of the fixator as aligned for the x-ray.
At step 630, the image processing set-up occurs. To facilitate the edge detection at step 520, the image contrast is increased. For example, a pixel with an intensity value that exceeds a threshold value, such as 155, would be increased to a value of 255, a maximum value. A pixel whose intensity does not exceed the threshold would have its intensity decreased by an order of magnitude. For example, a pixel with an intensity value of 100 would have the value decreased to a value of 10.
At step 640, set-up parameters for determining the location of circular images within the digital x-ray files are established. These parameters include the slope value used at step 520 to detect image edges, for example a value of 0.75, and minimum and maximum circle diameter values, used to filter circular images that would be too large or too small to represent the images generated from the projecting of the balls on the imaging device. Following this step, the process 510 moves to step 520 of process 210b.
The closer the ratio of the sum of the products of the lengths of the opposite sides of the quadrilateral to the product of the lengths of the diagonals is 1, the more likely a circular shape passes through the four points of interest. As such, images determined at step 530 that do not reach a threshold value for cyclicity could be screened from further processing. Alternatively, all images can be further processed to confirm that they are or are not circular images.
The quadrilateral generated by each set of five points is used to create four triangles. Each triangle is used to calculate the radius of a circle that would circumscribe the triangle.
Once the radius of the circumscribed circle about the four triangles is determined at step 910, then the circles' centers are determined, at step 920. To accomplish this determination, three angles are calculated based on the geometry of the four triangles depicted in
Once angle θ is calculated, the expressions below are used to determine the center of the circle. Expression I represent the rotation matrixes for the AP x-ray images taken positive counter clockwise about an axis normal to the plane of the image. A similar expression would be developed for the lateral x-ray. In the expressions provided below, the axis normal to the plane of the x-ray is the “Z” axis. Expression J is the starting direction of a vector having a magnitude equal to the radius of the circumscribed circle for the AP x-ray image. Again, a similar expression would be developed for the lateral x-ray. Expression K is the origin for the vector J that is to be rotated through the angle θ to arrive at the circumscribed circle's center. Expressions I, J and K use the subscript 0, 1, 2, and 3 to relate to the four triangles illustrated in
At step 930, the images are filtered. First, the mean and variance for the radius of each circular image is determined, based on the four calculated values for each triangle. Then, the mean values are compared to maximum and minimum values set for the analysis. Any image with a radius below a minimum or above a maximum value are not considered further. These maximum and minimum values are based on the expected size of the circular images to be formed by the imaging devices attached to the fixator.
At step 940, the images on the AP x-ray are then sorted by the x and y coordinates of the image circle centers, as calculated above (or, for the lateral x-ray, by the y and z coordinates). The coordinates of each circle center locations are compared to other circle center locations. Values for these locations that are within a certain tolerance level are determined to represent the same circle. In these cases, the data for these same circles are averaged together to get a mean center location for that circular image.
At step 940, an additional refinement is performed. The possible circular images are evaluated using a polar coordinate system. The image is evaluated at a distance equal to the radius as calculated for the circular image from the center location. As the evaluation steps around a circle, for example in increments of 22.5 degrees, the image should have an intensity value of 255 at each point a distance equal to the radius away from the center. This refinement confirms that the image is a circle, and not, for example, a square, which might have passed earlier filters.
In an alternative embodiment, the possible circular images corresponding to balls on an imaging device may be identified by a user, such as by using a pointing device and a graphical user interface (GUI). A user could use the pointing device to click on a point inside a circle. This step could be used to speed computations, by manually filtering the images. This step could also be used If the quality of the x-ray prevents proper identification of the images associated with the imaging device.
At step 1320, the slope and vertical intercepts for the anatomical axes are determined. This determination is made using the basic line equation, y=m×+b, where “m” is the slope of the line and “b” is the vertical, or “y” intercept. At step 1330, an image of each line representing the anatomical axes are superimposed onto the x-ray images to confirm the analysis. The process 560 then moves to step 570 of process 210b.
At step 1520, scaling factors are calculated for the two x-ray images. The physical orientation of the x-ray machine and medium, such as film, may cause the size of projected images to differ from the actual size of the structure that formed the image. The scaling factor is the ratio of the sum of the diameters of the six balls as measured by the process described above and the actual sum of the diameters of the six balls.
At step 540, the center and radius of the circular images on the x-rays as a result of the imaging device are determined. For the AP x-ray, the x and y coordinates of the ball centers were determined. From the lateral x-ray, the y and z coordinates were determined. Since two values for the y coordinate for each circle was determined, an offset for the lateral x-ray, as compared to the AP x-ray, can be determined. This determination is made at step 1530, with the offset value set to the average of the offsets for the six circle centers.
At step 1540, unit vectors for each of the balls on the imaging devices are determined. One endpoint of a unit vector is the circle center. The length of the vector is the length of the rod connecting the ball to the common point on the imaging device. At step 1550, a simultaneous solution of the equations representing the vectors allows for the origin, or common point, for each imaging device to be located on the digital image. In an alternative embodiment, a fourth ball could be located at the origin, and this step skipped.
At step 1560, the orthogonality of the system can be checked. Possible distortion of the x-ray image may cause the image from the imaging device to not be orthogonal. In this step, the orthogonality is check and the distortion noted. If the distortion level exceeds a threshold value, then the images may be corrected, using the orientation of the circular images of the imaging device to serve as the model for adjusting the image. The process 570 then moves to step 580 of process 210b.
At step 1730, the equations for each anatomical axis for each fragment is again calculated, based on the manipulated matrixes. To determine the equation of the anatomic axis for each of the bone fragments, proximal and distal, first, the equation of a plane that is normal to the AP x-ray image within which the proximal fragment anatomic axis lies is determined. Also determine is the equation of a plane that is normal to the AP x-ray image within which the distal fragment anatomic axis lies. The same process is repeated for the lateral x-ray. Then the intersection of the pair of planes corresponding to each fragment is taken and the equation of a line that is co-linear with the anatomic axis of the subject fragment is computed.
At step 1740, the axial rotation of the fragments is determined. Since the x-ray characterization algorithm cannot ascertain the axial rotation of the fragments an assumption could be made that both anterior anatomic markers, if present, the lines of which could be projected onto a plane normal to both the AP and lateral x-rays, would have the projected lines pointing in a directly anterior direction. An anatomical marker is a reference structure in the body associated with the bone fragment struction or other tissue structure. Anatomic markers would be, for instance, a foot for a distal fragment and a knee cap for a proximal fragment. Since this situation is not always the case, a clinical evaluation of one fragment's rotation relative to the other would generally be made, with the observation being made along the axis of one of the fragments with the anatomic marker of the other being projected onto a plane that would be normal to the anatomic axis of the reference fragment. This observed angulation would then be used to transform the coordinate system describing the other fragment, which initially would have a zero axial rotation value.
One skilled in the art would appreciate that the technique of process 210b, as described in
One skilled in the art would appreciate that the present invention supports a method for determining the proper configuration of a fixator or other medical device to correct a given deformity by solving the simultaneous equations representing the kinematic chain for the device. One skilled in the art would also appreciate that x-rays, clinical evaluations, or a combination of both may be used to determine the distal and proximal mounting characteristics, including the use of digital x-rays with images from an imaging device to reduce or eliminate the needs for a physician to take measurements. The technique can be expanded to other medical evaluations.
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